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. 1999 Oct;67(10):5012–5020. doi: 10.1128/iai.67.10.5012-5020.1999

FIG. 5.

FIG. 5

Nucleotide sequence of the IS1126 elements isolated in this study and the transposition site of IS11262. (A) Comparison of the nucleotide sequences and the deduced amino acid sequences of different IS1126 elements. Partial nucleotide and amino acid sequences of IS1126Tn were compared with those of IS1126 from P. gingivalis W83 and IS11262. Boxes represent the 12-bp terminal inverted repeats of IS1126. The 5-bp nucleotide sequences flanking inverted repeats are duplicated target sequences generated after IS1126 transposition. Asterisks denote the 4-bp 5′-GAAG-3′ deletion found in IS1126Tn which resulted in premature termination of IS1126 transposase synthesis. (B) Location of the duplicated copy of IS11262 found in P. gingivalis MSM-3 genome. A 4-kb BamHI restriction fragment (shaded) was cloned directly from MSM-3 chromosomal DNA into pGEM3Zf, and the nucleotide sequence was determined. Large arrows represent the size and orientation of the prtT, sod, prtC, and hmuR genes and of orfA. Small arrow in IS11262 indicates the direction of IS1126 transposase gene. prtT, cysteine protease gene; sod, superoxide dismutase gene; prtC, putative collagenase gene.